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US6353087B1 - Process for stripping polymer dispersions - Google Patents

Process for stripping polymer dispersions Download PDF

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US6353087B1
US6353087B1 US09/641,166 US64116600A US6353087B1 US 6353087 B1 US6353087 B1 US 6353087B1 US 64116600 A US64116600 A US 64116600A US 6353087 B1 US6353087 B1 US 6353087B1
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stripping
reaction composition
polymer
process according
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I-Hwa Midey Chang-Mateu
James Michael Lipovsky
Dawn Marie McFadden
Richard Shu-Hua Wu
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Rohm and Haas Co
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    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F6/00—Post-polymerisation treatments
    • C08F6/06—Treatment of polymer solutions
    • C08F6/10—Removal of volatile materials, e.g. solvents
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F6/00—Post-polymerisation treatments
    • C08F6/001—Removal of residual monomers by physical means
    • C08F6/003—Removal of residual monomers by physical means from polymer solutions, suspensions, dispersions or emulsions without recovery of the polymer therefrom
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F6/00—Post-polymerisation treatments
    • C08F6/006—Removal of residual monomers by chemical reaction, e.g. scavenging
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L15/00—Compositions of rubber derivatives

Definitions

  • This invention relates to a process for removing volatile organic compounds (“VOCs”) and amines such as ammonia from reaction compositions of polymer dispersions (“stripping”).
  • VOCs volatile organic compounds
  • amines such as ammonia
  • the invention relates to a process for stripping polymer dispersions which reduces gel in the polymer dispersion.
  • Polymers may be made by various processes, including solution, suspension, and emulsion polymerization.
  • dispersion is meant an emulsion or suspension polymer.
  • VOC is meant any volatile organic compound, such as residual monomers, impurities from monomers, and solvents from surfactants or monomers. Residual monomer is monomer that does not react during a polymerization and remains in the polymer dispersion. VOCs tend to have strong odors. Generally, people can smell VOCs at extremely low levels, such as in the part per million range. Some VOCs are toxic. Due to the toxicity of some VOCs and the fact that the smell of VOCs tends to be irritating, polymer dispersions generally are either chemically “chased” or stripped of VOCs.
  • Chemical chasing involves adding chemicals that react with unreacted monomers, such as tertiary butyl hydroperoxide, ammonium persulfate, potassium persulfate, or sodium persulfate which, for example may react with carbon-carbon double bonds of the unreacted monomers. Although chasing results in reduced residual monomers in the polymer latex, the level of residual monomers may still be unacceptably high. Also, any VOCs which do not have carbon-carbon double bonds can not be chased. Therefore, chemical chasing is sometimes followed by stripping to remove unreacted VOCs.
  • unreacted monomers such as tertiary butyl hydroperoxide, ammonium persulfate, potassium persulfate, or sodium persulfate which, for example may react with carbon-carbon double bonds of the unreacted monomers.
  • Stripping is a process wherein a dispersion is heated and a gas is sparged through the dispersion to remove VOCs. Stripping may also utilize vacuum to enable the stripping to be performed at lower temperatures.
  • the advantage to stripping polymer dispersions is that one can achieve lower levels of VOCs by stripping than by chasing.
  • Gel may form during the stripping process.
  • Gel is an aggregation of polymer particles or molecules, resulting in small clumps of polymer in the polymer solution or dispersion. Gel may cause problems in down stream applications, therefore there is a need for a polymer dispersion stripping process which reduces gel formation.
  • a second problem associated with stripping polymer dispersions is that the polymer dispersions frequently contain surfactants.
  • Polymers may also behave as surfactants due to carboxy end groups.
  • the surfactants or surfactant behavior of a polymer may cause foaming during stripping operations. Foaming may be controlled through the addition of chemicals such as silicone, mineral and vegetable oils, ethoxylated fatty acids, and alcohols.
  • chemicals may be expensive and the chemicals may adversely effect the polymer properties, for example, the chemicals may cause surface imperfections such as fish eyes or holes in coatings.
  • a process for foam destruction in the manufacturing of polymers was disclosed in European Patent Application EP 865811.
  • the process utilized mechanical foam breakers to destroy foam during the process of manufacturing a polymer.
  • the process did not address the issue of gel formation during a polymer solution or dispersion stripping process.
  • U.S. Pat. No. 4,130,527 disclosed a stripping process which utilized a continuous stripping operation. Steam was fed counter-current to a falling film of polymer. The disclosure did not address the problems of foaming or gel formation during stripping polymer dispersions or solutions.
  • the present invention provides a process including: providing a reaction composition and stripping the reaction composition in the presence of a mechanical foam breaker and an agitator; wherein the reaction composition is treated by a method selected from: a) adjusting the pH to from 7 to 11 prior to stripping and maintaining the adjusted pH during stripping, b) maintaining the temperature of the reaction composition at from 30° C. to 70° C. during stripping, and c) combinations thereof.
  • the first step in the process of the invention involves providing a reaction composition.
  • the reaction composition may be polymers may be made by suspension or emulsion polymerization. Polymers made by emulsion polymerization are preferred. The polymers may be homopolymers or copolymers.
  • ethylenically unsaturated monomers which include, but are not limited to (meth)acrylic ester monomers including methyl acrylate, ethyl acrylate, butyl acrylate, 2-ethylhexyl acrylate, decyl acrylate, methyl methacrylate, butyl methacrylate, hydroxyethyl methacrylate, and hydroxypropyl acrylate; acrylamide or substituted acrylamides; styrene or substituted styrene; vinyl acetate or other vinyl esters; vinyl monomers such as vinyl chloride, vinylidene chloride, N-vinyl pyrolidone; and acrylonitrile or methacrylonitrile. Butyl acrylate, methyl methacrylate, and styrene are preferred.
  • Ethylenically unsaturated acid containing monomers or salts thereof may also be useful.
  • Suitable ethylenically unsaturated acid containing monomers include, but are not limited to acrylic acid, methacrylic acid, crotonic acid, phosphoethyl methacrylate, 2-acrylamido-2-methyl-1-propanesulfonic acid, sodium vinyl sulfonate, itaconic acid, fumaric acid, maleic acid, monomethyl itaconate, monomethyl fumarate, monobutyl fumarate, and maleic anhydride.
  • Acrylic acid and methacrylic acid are preferred. Methacrylic acid is more preferred.
  • a fluorinated (meth)acrylate ethylenically unsaturated monomer such as ZonylTM products (Trademark of DuPont Chemical Company) may also be useful.
  • a silicone containing ethylenically unsaturated monomer such as vinyl trimethoxy silane and methacryloxy propyl trimethoxy silane may also be useful.
  • Monomers selected from C 6 -C 20 alkyl styrene and alkyl-alpha-methyl styrene, C 6 -C 20 alkyl dialkyl itaconate, C 10 -C 20 vinyl esters of carboxylic acids, C 8 -C 20 N-alkyl acrylamide and methacrylamide, C 10 -C 20 alkyl alpha-hydroxymethylacrylate, C 8 -C 20 dialkyl 2,2′-(oxydimethylene) diacrylate, C 8 -C 20 dialkyl 2,2′-(alkyliminodimethylene)diacrylate, C 8 -C 20 N-alkylacrylimide, and C 10 -C 20 alkyl vinylether may also be useful.
  • Hydrophobic monomers such as C 12 to C 40 alkyl ester of (meth)acrylic acid may also be useful.
  • Suitable alkyl esters of (meth)acrylic acid include, but are not limited to lauryl (meth)acrylate, cetyl (meth)acrylate, stearyl (meth)acrylate, behenyl (meth)acrylate, and eicosyl (meth)acrylate.
  • Emulsion polymerizations are well known in the art and are described in U.S. Pat. No. 5,346,954, hereby incorporated by reference. Suitable initiators and process conditions can be found in the patent.
  • the process of the invention yields a polymer dispersion with reduced gel.
  • the formation of gel may be reduced by adjusting the pH of the reaction composition to from 7 to 11, preferably from 8 to 11, more preferably from 9 to 11 prior to stripping.
  • the pH of the reaction composition is then maintained during stripping.
  • the pH adjustment and maintenance may be achieved through the addition of base, such as, but not limited to sodium hydroxide, potassium hydroxide, or ammonium hydroxide. Where removal of amine odors is desired, potassium hydroxide or sodium hydroxide are preferred bases.
  • the formation of gel may also be reduced through reducing the temperature of the reaction composition during stripping.
  • Stripping in a batch mode involves heating the solution or dispersion in a reactor and sparging a gas through the dispersion to remove VOCs. Vacuum may be applied to the reactor to allow stripping to occur at lower temperatures.
  • Stripping of the reaction composition may be performed at a temperature ranging from 30° C. to 70° C., preferably 40° C. to 70° C., more preferably 45 to 59° C.
  • the vacuum may range from 20 mmHg to 150 mmHg, preferably from 40 mm Hg to 120 mm Hg, more preferably from 60 mm Hg to 100 mm Hg.
  • the gas utilized for stripping may be steam, nitrogen, helium, humid or wet air, wet nitrogen, or wet helium.
  • humid or wet is meant that the gas contains water vapor.
  • pH adjustment and temperature control may be desirable to combine pH adjustment and temperature control during the stripping of a reaction composition.
  • the temperature and pH ranges described above are useful when both temperature and pH control are utilized in a polymer solution or dispersion stripping operation.
  • the amount of gas holdup in the polymer dispersion effects the rate at which the VOC's are removed. Agitation effects the gas holdup.
  • the rate at which VOCs are removed from the polymer dispersion may be improved through the use of concave-blade disc impellers, a radial agitator, as described by Bakker et al. in Chemical Engineering (December 1994), p. 98-104.
  • Another method suitable for improving the rate at which VOCs are removed from the polymer dispersion is to change the direction of pumping of the agitators, such as, but not limited to pitched blade turbines so that the reaction composition is pumped up in the reactor.
  • a continuous stripping process may be desired. Therefore, in a second embodiment of the present invention, there is provided a process including: continuously feeding a reaction composition selected from an acrylic solution polymer and an acrylic dispersion polymer containing volatile organic compounds down a stripping column having a top and a bottom; ii) continuously feeding steam up from the bottom of the stripping column; and iii) removing the volatile organic compounds from the polymer.
  • the reaction composition is an acrylic solution polymer or an acrylic dispersion polymer and the stripping is performed in a continuous mode.
  • an acrylic solution or dispersion polymer is continuously fed to a stripping column.
  • the polymer solution or dispersion falls down the column, creating a thin film of polymer along the column walls.
  • Steam is simultaneously fed up the column.
  • Volatile organic compounds are removed from the polymer in the column.
  • the process may be operated under the same temperature and pressure conditions as the batch mode described above.
  • the column flux rate of acrylic solution or dispersion polymer into the column may range from 2,500 kg per hour per m 2 to 30,000 kg per hour per m 2 , preferably from 7,500 kg per hour per m 2 to 25,000 kg per hour per m 2 .
  • the column flux rate of steam into the column may range from 500 kg per hour per m 2 to 12,500 kg per hour per m 2 , preferably from 1,500 kg per hour per m 2 to 10,000 kg per hour per m 2 , more preferably from 2,500 kg per hour per m 2 to 5,000 kg per hour per m 2 .
  • the ratio of steam fed to polymer solution or dispersion fed to the column may range from 0.1 to 0.6, preferably from 0.15 to 0.45, more preferably from 0.2 to 0.3. Maintaining the ratio of steam fed to polymer solution or dispersion fed to the column in this range helps to prevent foam generation.
  • gel formation may be controlled as discussed above in the first aspect of the invention, such as pH adjustment and temperature control.
  • the amount of the redox system combination added to the polymer solution or dispersion typically ranges from 0.01 wt % to 0.5 wt %, preferably 0.05 wt % to 0.4 wt %, more preferably 0.2 wt % to 0.3 wt %, based on the total weight of the monomers used in the polymerization.
  • Inisurfs may contain both hydrophilic and hydrophobic groups.
  • hydrophilic groups include polyethylene oxide, carboxylate, or sulfonate groups.
  • An example of a hydrophobic group is a paraffin group.
  • Inisurfs may be prepared by linking paraffin radicals having 10 to 18 carbon atoms with azo compounds, such as paraffin sulfochlorides or paraffin disulfonic acid chloride with azo compounds containing one or two iminoether or amidine groups.
  • Alternative inisurfs may be prepared by reacting hydroperoxides or hydrogen peroxide with cyclic acid anhydrides of carboxylic acids or sulfonic acids containing 12 to 30 carbon atoms.
  • autoxidizable compounds include wood oil, tall oil, tung oil, safflower oil, lallementia oil, linseed oil, oiticica oil, perilla oil, poppyseed oil, sesame seed oil, walnut oil, hempseed oil, or castor oil.
  • the compounds may also be modified with polyethylene oxide.
  • the amount of inisurf added to the polymer solution or dispersion typically ranges from 0.05 wt % to 10 wt %, preferably 0.1 wt % to 2 wt %, based on the total weight of the monomers used in the polymerization.
  • Nucleophiles may also be useful as chemical chasers. Suitable nucleophiles include, but are not limited to thiols, thio ureadioxide, sulfides, hydrogen sulfide, salts of sulfinic acid, sulfenic acid, disulfides such as sodium sulfide, sodium bisulfide, sodium thiosulfate, sodium sulfite, sodium bisulfite, sodium dioxide, phosphanes, alkylphosphanes, triphenyl phosphane, aminophosphanes, phosphorous acid and salts thereof, hypophosphorous acid and salts thereof, ammonia, primary and secondary amines, oximes, hydroxylamines, hydroxamic acids, hydrazine, and substituted hydrazines.
  • thiols such as sodium sulfide, sodium bisulfide, sodium thiosulfate, sodium sulfite, sodium bisul
  • the molar ratio of nucleophile added to residual monomer typically ranges from 0.5 mole to 5 mole per mole monomer, preferably 0.9 mole to 3 mole, more preferably 0.9 mole to 2 mole nucleophile per mole residual monomer.
  • Organic carboxylic acids which contain no polymerizable olefinically unsaturated C—C double bonds and have a molecular weight of not more than 300 may also be useful as chemical chasers in aqueous polymer dispersions where a redox initiator system is concurrently utilized.
  • the redox initiator added is separate from the initiator system utilized to begin the polymerization.
  • the organic carboxylic acids may be aliphatic carboxylic acids with 1 to 20 and preferably 1 to 8 carbon atoms, having a water solubility of greater than 20 g per liter of water.
  • Suitable organic carboxylic acids include, but are not limited to formic acid, benzoic acid, monochloroacetic acid, trifluoroacetic acid, naphthalenecarboxylic acid, oxalic acid, succinic acid, adipic acid, phthalic acid, terephthalic acid, derivatives thereof, and salts thereof.
  • the polyvalent metal ion may be selected from iron, copper, manganese, vanadium, nickel, cerium, chromium, platinum, and palladium. Iron and manganese are preferred.
  • the amount of the redox initiator system may range from 0.01 weight percent to 10 weight percent, preferably from 0.01 weight percent to 5 weight percent, based on the monomers used.
  • a batch steam stripping apparatus was set up including a 20 liter vessel equipped with a heated jacket, an agitator, an EKATO Foamjet, a vacuum source controlled by a needle valve, an electronic controller for the vacuum, an overhead condenser, and a steam sparger.
  • the pressure was controlled near the water vapor-liquid equilibrium at a given temperature.
  • To the vessel was added 11,000 g polymer dispersion which was chemically chased by one of the methods described above.
  • the pH of the polymer was either unadjusted, or adjusted with sodium hydroxide or ammonium hydroxide.
  • Steam was purged through the steam sparger at a rate of 10 g per minute.
  • the EKATO Foamjet was rotated at a rate of 3,350 rotations per minute.
  • the stripping process was run for approximately four hours.
  • Two commercially available butyl acrylate/methyl methacrylate polymers were steam stripped at various temperatures in degrees C, pressures in mmHg, and pHs as indicated in
  • the polymers had been chemically chased by the following process based on a total batch size of 13,500 g: Following the conversion of 90-99.99% of ethylenically unsaturated monomer to polymer, the polymer was cooled to 60° C. To the cooled polymer was added 80 ml of a charge promoter solution (0.15% FeSO 4 .H 2 O in water). The polymer was stirred for approximately 15 minutes. A charge catalyst solution containing 8 g tertiary butyl hydroperoxide in 56 ml water was then added to the polymer. The polymer was stirred for approximately 15 minutes. A charge activator solution containing 8 g isoascorbic acid in 160 ml water was then added to the polymer. The polymer was stirred for approximately 15 minutes. After chemical chasing, the polymer dispersions were steam stripped.
  • a charge promoter solution 0.15% FeSO 4 .H 2 O in water
  • emulsion polymers were continuously stripped using two different sets of stripping equipment.
  • the first set of equipment was a Buffalo Technologies Corporation falling film stripper.
  • the column had an internal diameter of 5.1 cm and a length of 3.7 m.
  • the emulsion polymers were fed down the column while steam was fed up the column. Stripping was performed both under vacuum and at atmospheric pressure (Wet Air Stripping).
  • the polymers were measured for VOCs by Gas Chromatography both before and after stripping. VOCs with boiling points below 100° C. were combined and reported together, as were VOCs with boiling points above 100° C.
  • the samples were also passed through a 325 mesh screen to test for gel formation. The results of these experiments are shown in Table 3.
  • the initial VOC levels for polymer A were 1342 ppm with a boiling point ⁇ 100 ° C. and 432 ppm with a boiling point >100° C.
  • the initial VOC levels for polymer B were 477 ppm with a boiling point ⁇ 100° C., and 605 ppm with a boiling point >100° C.
  • the examples above show that the continuous process utilizing the Buffalo Technologies Corporation falling film column removed VOCs from the polymer dispersion and did not form gel.

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  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Dispersion Chemistry (AREA)
  • General Chemical & Material Sciences (AREA)
  • Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
  • Processes Of Treating Macromolecular Substances (AREA)
  • Degasification And Air Bubble Elimination (AREA)

Abstract

This invention relates to a process for stripping polymer reaction compositions. The process reduces gel in the polymer reaction composition by adjusting the pH of the polymer to from 7 to 11 prior to stripping and maintaining the adjusted pH during stripping, maintaining the temperature of the polymer at from 30° C. to 70° C. during stripping, utilizing a continuous stripping operation, or combinations thereof.

Description

This appln claims benefit of provisional application No. 60/151,096 filed Aug. 27, 1999.
This invention relates to a process for removing volatile organic compounds (“VOCs”) and amines such as ammonia from reaction compositions of polymer dispersions (“stripping”). In particular, the invention relates to a process for stripping polymer dispersions which reduces gel in the polymer dispersion.
Polymers may be made by various processes, including solution, suspension, and emulsion polymerization. As used herein, by dispersion is meant an emulsion or suspension polymer. Although the polymerization processes are efficient, there is always some VOCs after the polymerization is complete. As used herein, by VOC is meant any volatile organic compound, such as residual monomers, impurities from monomers, and solvents from surfactants or monomers. Residual monomer is monomer that does not react during a polymerization and remains in the polymer dispersion. VOCs tend to have strong odors. Generally, people can smell VOCs at extremely low levels, such as in the part per million range. Some VOCs are toxic. Due to the toxicity of some VOCs and the fact that the smell of VOCs tends to be irritating, polymer dispersions generally are either chemically “chased” or stripped of VOCs.
Chemical chasing involves adding chemicals that react with unreacted monomers, such as tertiary butyl hydroperoxide, ammonium persulfate, potassium persulfate, or sodium persulfate which, for example may react with carbon-carbon double bonds of the unreacted monomers. Although chasing results in reduced residual monomers in the polymer latex, the level of residual monomers may still be unacceptably high. Also, any VOCs which do not have carbon-carbon double bonds can not be chased. Therefore, chemical chasing is sometimes followed by stripping to remove unreacted VOCs.
Stripping is a process wherein a dispersion is heated and a gas is sparged through the dispersion to remove VOCs. Stripping may also utilize vacuum to enable the stripping to be performed at lower temperatures. The advantage to stripping polymer dispersions is that one can achieve lower levels of VOCs by stripping than by chasing.
One problem associated with stripping polymer dispersions is that gel may form during the stripping process. Gel is an aggregation of polymer particles or molecules, resulting in small clumps of polymer in the polymer solution or dispersion. Gel may cause problems in down stream applications, therefore there is a need for a polymer dispersion stripping process which reduces gel formation.
A second problem associated with stripping polymer dispersions is that the polymer dispersions frequently contain surfactants. Polymers may also behave as surfactants due to carboxy end groups. The surfactants or surfactant behavior of a polymer may cause foaming during stripping operations. Foaming may be controlled through the addition of chemicals such as silicone, mineral and vegetable oils, ethoxylated fatty acids, and alcohols. Two disadvantages of chemical addition to control foaming are that the chemicals may be expensive and the chemicals may adversely effect the polymer properties, for example, the chemicals may cause surface imperfections such as fish eyes or holes in coatings.
Mechanical foam breakers may also be utilized to reduce foam during polymer dispersion stripping operations, however the foam breaker does not reduce the formation of gel in the polymer dispersion. Therefore, there is also a need for a polymer dispersion stripping process which prevents foam formation or destroys foam generated during stripping.
One approach to controlling foam generation during a polymer dispersion stripping process was taught in German unexamined patent application DE 19517680. The process disclosed in that patent required pH adjustment to the range of from 5 to 6.8 during stripping to reduce foam generation. After stripping, the pH was adjusted to from 8 to 10. The process did not utilize a mechanical foam breaker and did not deal with the issue of gel formation during stripping.
A process for foam destruction in the manufacturing of polymers was disclosed in European Patent Application EP 865811. The process utilized mechanical foam breakers to destroy foam during the process of manufacturing a polymer. The process did not address the issue of gel formation during a polymer solution or dispersion stripping process.
U.S. Pat. No. 4,130,527 disclosed a stripping process which utilized a continuous stripping operation. Steam was fed counter-current to a falling film of polymer. The disclosure did not address the problems of foaming or gel formation during stripping polymer dispersions or solutions.
Despite the disclosure of the references, there is a continuing need for a process for stripping polymer dispersions wherein foam formation is prevented or foam formed during stripping is destroyed and gel formation is minimized.
The present invention provides a process including: providing a reaction composition and stripping the reaction composition in the presence of a mechanical foam breaker and an agitator; wherein the reaction composition is treated by a method selected from: a) adjusting the pH to from 7 to 11 prior to stripping and maintaining the adjusted pH during stripping, b) maintaining the temperature of the reaction composition at from 30° C. to 70° C. during stripping, and c) combinations thereof.
As indicated above, the first step in the process of the invention involves providing a reaction composition. The reaction composition may be polymers may be made by suspension or emulsion polymerization. Polymers made by emulsion polymerization are preferred. The polymers may be homopolymers or copolymers.
Among the monomers that may be useful to make the polymer dispersion are ethylenically unsaturated monomers which include, but are not limited to (meth)acrylic ester monomers including methyl acrylate, ethyl acrylate, butyl acrylate, 2-ethylhexyl acrylate, decyl acrylate, methyl methacrylate, butyl methacrylate, hydroxyethyl methacrylate, and hydroxypropyl acrylate; acrylamide or substituted acrylamides; styrene or substituted styrene; vinyl acetate or other vinyl esters; vinyl monomers such as vinyl chloride, vinylidene chloride, N-vinyl pyrolidone; and acrylonitrile or methacrylonitrile. Butyl acrylate, methyl methacrylate, and styrene are preferred.
Ethylenically unsaturated acid containing monomers or salts thereof may also be useful. Suitable ethylenically unsaturated acid containing monomers include, but are not limited to acrylic acid, methacrylic acid, crotonic acid, phosphoethyl methacrylate, 2-acrylamido-2-methyl-1-propanesulfonic acid, sodium vinyl sulfonate, itaconic acid, fumaric acid, maleic acid, monomethyl itaconate, monomethyl fumarate, monobutyl fumarate, and maleic anhydride. Acrylic acid and methacrylic acid are preferred. Methacrylic acid is more preferred.
A fluorinated (meth)acrylate ethylenically unsaturated monomer, such as Zonyl™ products (Trademark of DuPont Chemical Company) may also be useful.
A silicone containing ethylenically unsaturated monomer, such as vinyl trimethoxy silane and methacryloxy propyl trimethoxy silane may also be useful.
Monomers selected from C6-C20 alkyl styrene and alkyl-alpha-methyl styrene, C6-C20 alkyl dialkyl itaconate, C10-C20 vinyl esters of carboxylic acids, C8-C20 N-alkyl acrylamide and methacrylamide, C10-C20 alkyl alpha-hydroxymethylacrylate, C8-C20 dialkyl 2,2′-(oxydimethylene) diacrylate, C8-C20 dialkyl 2,2′-(alkyliminodimethylene)diacrylate, C8-C20 N-alkylacrylimide, and C10-C20 alkyl vinylether may also be useful.
Hydrophobic monomers such as C12 to C40 alkyl ester of (meth)acrylic acid may also be useful. Suitable alkyl esters of (meth)acrylic acid include, but are not limited to lauryl (meth)acrylate, cetyl (meth)acrylate, stearyl (meth)acrylate, behenyl (meth)acrylate, and eicosyl (meth)acrylate.
Emulsion polymerizations are well known in the art and are described in U.S. Pat. No. 5,346,954, hereby incorporated by reference. Suitable initiators and process conditions can be found in the patent.
In one aspect of the present invention, polymers are stripped in the presence of a mechanical foambreaker. Mechanical foambreakers are described by M. Zlokarnik in Chem. Ing. Tech. 56 (1984), p. 839-844, hereby incorporated by reference for the types of foambreakers that may be useful in the process on the invention. Suitable foambreakers include, but are not limited to cyclones, Franz rotators, the EKATO Foamjet through the EKATO Company of Ramsey, N.J., and the FUNDAFOM® foam destroyer through Chemap AG of Volketswil, Switzerland.
The process of the invention yields a polymer dispersion with reduced gel. The formation of gel may be reduced by adjusting the pH of the reaction composition to from 7 to 11, preferably from 8 to 11, more preferably from 9 to 11 prior to stripping. The pH of the reaction composition is then maintained during stripping. The pH adjustment and maintenance may be achieved through the addition of base, such as, but not limited to sodium hydroxide, potassium hydroxide, or ammonium hydroxide. Where removal of amine odors is desired, potassium hydroxide or sodium hydroxide are preferred bases.
The formation of gel may also be reduced through reducing the temperature of the reaction composition during stripping. Stripping in a batch mode involves heating the solution or dispersion in a reactor and sparging a gas through the dispersion to remove VOCs. Vacuum may be applied to the reactor to allow stripping to occur at lower temperatures.
Stripping of the reaction composition may be performed at a temperature ranging from 30° C. to 70° C., preferably 40° C. to 70° C., more preferably 45 to 59° C. The vacuum may range from 20 mmHg to 150 mmHg, preferably from 40 mm Hg to 120 mm Hg, more preferably from 60 mm Hg to 100 mm Hg.
The gas utilized for stripping may be steam, nitrogen, helium, humid or wet air, wet nitrogen, or wet helium. As used herein, by humid or wet is meant that the gas contains water vapor.
It may be desirable to combine pH adjustment and temperature control during the stripping of a reaction composition. The temperature and pH ranges described above are useful when both temperature and pH control are utilized in a polymer solution or dispersion stripping operation.
We have also discovered that the amount of gas holdup in the polymer dispersion effects the rate at which the VOC's are removed. Agitation effects the gas holdup. The rate at which VOCs are removed from the polymer dispersion may be improved through the use of concave-blade disc impellers, a radial agitator, as described by Bakker et al. in Chemical Engineering (December 1994), p. 98-104. Another method suitable for improving the rate at which VOCs are removed from the polymer dispersion is to change the direction of pumping of the agitators, such as, but not limited to pitched blade turbines so that the reaction composition is pumped up in the reactor.
For various reasons, a continuous stripping process may be desired. Therefore, in a second embodiment of the present invention, there is provided a process including: continuously feeding a reaction composition selected from an acrylic solution polymer and an acrylic dispersion polymer containing volatile organic compounds down a stripping column having a top and a bottom; ii) continuously feeding steam up from the bottom of the stripping column; and iii) removing the volatile organic compounds from the polymer.
In this second embodiment of the present invention, the reaction composition is an acrylic solution polymer or an acrylic dispersion polymer and the stripping is performed in a continuous mode. In the continuous mode, an acrylic solution or dispersion polymer is continuously fed to a stripping column. The polymer solution or dispersion falls down the column, creating a thin film of polymer along the column walls. Steam is simultaneously fed up the column. Volatile organic compounds are removed from the polymer in the column. The process may be operated under the same temperature and pressure conditions as the batch mode described above.
The column flux rate of acrylic solution or dispersion polymer into the column may range from 2,500 kg per hour per m2 to 30,000 kg per hour per m2, preferably from 7,500 kg per hour per m2 to 25,000 kg per hour per m2. The column flux rate of steam into the column may range from 500 kg per hour per m2 to 12,500 kg per hour per m2, preferably from 1,500 kg per hour per m2 to 10,000 kg per hour per m2, more preferably from 2,500 kg per hour per m2 to 5,000 kg per hour per m2. The ratio of steam fed to polymer solution or dispersion fed to the column may range from 0.1 to 0.6, preferably from 0.15 to 0.45, more preferably from 0.2 to 0.3. Maintaining the ratio of steam fed to polymer solution or dispersion fed to the column in this range helps to prevent foam generation.
In the second embodiment of the invention, gel formation may be controlled as discussed above in the first aspect of the invention, such as pH adjustment and temperature control.
In another embodiment of the invention, the polymer dispersion is chemically chased prior to stripping. Suitable chemical chasers include redox system combinations of oxidizing agents such as, but not limited to water-soluble hydroperoxides, tertiary butyl hydroperoxide, cumene hydroperoxide, hydrogen peroxide, sodium peroxide, potassium peroxide, sodium perborate, potassium persulfate, sodium persulfate, ammonium persulfate, persulfuric acid and salts thereof, perphosphoric acid and salts thereof, potassium permanganate, and an ammonium or alkali salt of peroxydisulfuric acid; reducing agents, such as, but not limited to ascorbic acid, isoascorbic acid, organic compounds containing thiol or disulfide groups, reducing inorganic alkali and ammonium salts of sulfur-containing acids, such as sodium sulfite, disulfite, thiosulfate, hydrosulfite, sulfide, hydrosulfide or dithionite, formadinesulfinic acid, hydroxymethanesulfonic acid, acetone bisulfite, amines, such as ethanolamine, glycolic acid, glyoxylic acid hydrate, lactic acid, glyceric acid, malic acid, tartaric acid, and oxidizing agents that are gaseous under normal conditions, such as oxygen, ozone, or air, or gaseous reducing agents, such as sulfur dioxide; and redox reaction catalyzing metal salts of iron, copper, manganese, silver, platinum, vanadium, nickel, chromium, palladium, or cobalt.
The amount of the redox system combination added to the polymer solution or dispersion typically ranges from 0.01 wt % to 0.5 wt %, preferably 0.05 wt % to 0.4 wt %, more preferably 0.2 wt % to 0.3 wt %, based on the total weight of the monomers used in the polymerization.
Surface active initiators containing at least one hydroperoxide, peroxo, or azo group (known as inisurfs) may also be utilized. The compounds were reviewed by B. A. Guyot and K. Tauer in Adv. Polymer Sci., Vol. 111, pp 54-64, and by K. Tauer in Polymer News, 1995, Vol. 20, pp. 342-347, hereby incorporated by reference for suitable inisurfs useful for chemical chasing.
Inisurfs may contain both hydrophilic and hydrophobic groups. Examples of hydrophilic groups include polyethylene oxide, carboxylate, or sulfonate groups. An example of a hydrophobic group is a paraffin group.
Inisurfs may be prepared by linking paraffin radicals having 10 to 18 carbon atoms with azo compounds, such as paraffin sulfochlorides or paraffin disulfonic acid chloride with azo compounds containing one or two iminoether or amidine groups. Alternative inisurfs may be prepared by reacting hydroperoxides or hydrogen peroxide with cyclic acid anhydrides of carboxylic acids or sulfonic acids containing 12 to 30 carbon atoms.
Other useful compounds include hydroperoxide or peroxo-group containing compounds which are the products of oxidation or autoxidation of autoxidizable, olefinically unsaturated fatty acids, fatty acid compounds, or fatty alcohols or hydrocarbons. The autoxidizable compounds include wood oil, tall oil, tung oil, safflower oil, lallementia oil, linseed oil, oiticica oil, perilla oil, poppyseed oil, sesame seed oil, walnut oil, hempseed oil, or castor oil.
Oleic acid, linolenic acid, linoleic acid, ricinoleic acid, elaidic acid, soybean oil fatty acid, frucic acid, erucic acid, arachidonic acid, palmitoleic acid, petroselic acid, oleyl alcohol, as well as drying fatty acids and fatty alcohols, which were prepared by conjugating or isomerizing the natural fatty acids, are also suitable autoxidizable fatty acids, fatty alcohols and hydrocarbons. The compounds may also be modified with polyethylene oxide.
The amount of inisurf added to the polymer solution or dispersion typically ranges from 0.05 wt % to 10 wt %, preferably 0.1 wt % to 2 wt %, based on the total weight of the monomers used in the polymerization.
Nucleophiles may also be useful as chemical chasers. Suitable nucleophiles include, but are not limited to thiols, thio ureadioxide, sulfides, hydrogen sulfide, salts of sulfinic acid, sulfenic acid, disulfides such as sodium sulfide, sodium bisulfide, sodium thiosulfate, sodium sulfite, sodium bisulfite, sodium dioxide, phosphanes, alkylphosphanes, triphenyl phosphane, aminophosphanes, phosphorous acid and salts thereof, hypophosphorous acid and salts thereof, ammonia, primary and secondary amines, oximes, hydroxylamines, hydroxamic acids, hydrazine, and substituted hydrazines.
The molar ratio of nucleophile added to residual monomer typically ranges from 0.5 mole to 5 mole per mole monomer, preferably 0.9 mole to 3 mole, more preferably 0.9 mole to 2 mole nucleophile per mole residual monomer.
Organic carboxylic acids which contain no polymerizable olefinically unsaturated C—C double bonds and have a molecular weight of not more than 300 may also be useful as chemical chasers in aqueous polymer dispersions where a redox initiator system is concurrently utilized. In this embodiment of the invention, the redox initiator added is separate from the initiator system utilized to begin the polymerization. The redox initiator system typically comprises a peroxide or a peroxide generator at from 0.01 weight percent to 5 weight percent based on the total amount of monomers utilized for making the polymer dispersion, from 30 mole percent to 300 mole percent based on the peroxide or peroxide generator of an organic carboxylic acid described above, from 0 to 1000, preferably from 10 to 100 ppm based on the total amount of monomers utilized to prepare the polymer dispersion of a polyvalent metal ion capable of varying its valency, and from 0 to 10 weight percent based on the total amount of monomers utilized to prepare the polymer dispersion of a mineral acid.
The organic carboxylic acids may be aliphatic carboxylic acids with 1 to 20 and preferably 1 to 8 carbon atoms, having a water solubility of greater than 20 g per liter of water. Suitable organic carboxylic acids include, but are not limited to formic acid, benzoic acid, monochloroacetic acid, trifluoroacetic acid, naphthalenecarboxylic acid, oxalic acid, succinic acid, adipic acid, phthalic acid, terephthalic acid, derivatives thereof, and salts thereof.
The polyvalent metal ion may be selected from iron, copper, manganese, vanadium, nickel, cerium, chromium, platinum, and palladium. Iron and manganese are preferred.
The amount of the redox initiator system may range from 0.01 weight percent to 10 weight percent, preferably from 0.01 weight percent to 5 weight percent, based on the monomers used.
Throughout this specification and claims, unless otherwise indicated, references to percentages are by weight percent and all temperatures are in degree centigrade.
It is also to be understood that for purposes of this specification and claims that the range and ratio limits, recited herein, are combinable. For example, if ranges of 1-20 and 5-15 are recited for a particular parameter, it is understood that ranges of 1-15 or 5-20 are also contemplated.
The following examples are intended to illustrate the process of the invention. The examples should not be construed as limiting the scope of the invention.
EXAMPLE 1 Batch Steam Stripping
A batch steam stripping apparatus was set up including a 20 liter vessel equipped with a heated jacket, an agitator, an EKATO Foamjet, a vacuum source controlled by a needle valve, an electronic controller for the vacuum, an overhead condenser, and a steam sparger. The pressure was controlled near the water vapor-liquid equilibrium at a given temperature. To the vessel was added 11,000 g polymer dispersion which was chemically chased by one of the methods described above. The pH of the polymer was either unadjusted, or adjusted with sodium hydroxide or ammonium hydroxide. Steam was purged through the steam sparger at a rate of 10 g per minute. The EKATO Foamjet was rotated at a rate of 3,350 rotations per minute. The stripping process was run for approximately four hours. Two commercially available butyl acrylate/methyl methacrylate polymers were steam stripped at various temperatures in degrees C, pressures in mmHg, and pHs as indicated in Table 1.
The polymers had been chemically chased by the following process based on a total batch size of 13,500 g: Following the conversion of 90-99.99% of ethylenically unsaturated monomer to polymer, the polymer was cooled to 60° C. To the cooled polymer was added 80 ml of a charge promoter solution (0.15% FeSO4.H2O in water). The polymer was stirred for approximately 15 minutes. A charge catalyst solution containing 8 g tertiary butyl hydroperoxide in 56 ml water was then added to the polymer. The polymer was stirred for approximately 15 minutes. A charge activator solution containing 8 g isoascorbic acid in 160 ml water was then added to the polymer. The polymer was stirred for approximately 15 minutes. After chemical chasing, the polymer dispersions were steam stripped.
Samples of each polymer dispersion were tested before and after steam stripping for gel content. The test was run by passing 750 ml of polymer dispersion through a 325 mesh screen. Any gel on the screen was dried and the dry weight of gel per 750 ml of dispersion was calculated. Where the screen was overloaded with gel such that the entire sample could not be passed through the screen (binded), the sample was rated a failure and the gel was not measured. The results of the gel tests are reported in Table 1.
TABLE 1
pH Gel
Polymer Before After Temperature Before After
A 9.5 10. 53 0.02 0.01
A 9.8 8.6 54 0.02 0.05
A 9.0 7.4 54 Not Run Not Run*
B 4.7 4.7 58 0.02 Binded
B 4.5 4.5 50 0.02 0.16
B 4.4 4.2 47 0.03 0.06
B 9.1 8.5 49 0.02 0.02
B 9.1 8.7 55 0.02 0.08
*gels were not run on this sample - due to a large amount of gels remaining in the vessels after the run.
EXAMPLE 2 Comparison of Direction of Polymer Movement
These experiments were designed to show the effects of the direction of agitation during stripping on the rate of VOC removal from the polymer. The set up was the same as Example 1 except in Experiment 1, the agitator was 3 pitched blade turbines having a diameter equal to 28% of the reactor diameter. In this experiment, the agitator was pumping polymer down the reactor. In experiment 2, the agitator was 2 pitched blade turbines having a diameter equal to 48% of the reactor diameter. In this experiment, the agitator was pumping polymer up the reactor. Approximately 10,000 g of polymer emulsion were added to the stripping vessel. The polymer emulsion was heated to 50° C. Steam was introduced into the system at an average rate of 19.7 g/min. Experiment 3 was a repeat of Experiment 2, except the steam rate was decreased to 8.6 g/min. Samples were removed at 30 minute intervals and analyzed by gas chromatography for residual VOCs. The results of these experiments are shown in Table 2.
TABLE 2
Initial % VOC Retained Over Time (minutes)
Example VOC (ppm) 30 60 90 120 180 240
1 (Comp) 1205 NA 77 NA 60 41 33
2 1165 58 29 16  9  5  2
3 1351 61 48 39 31 23 17
Comp = comparative
The experiments above show that VOCs are removed from the polymers much faster when the direction of agitation is changed to pump the polymer up in the reactor, as opposed to the agitator pumping the polymer down the reactor.
EXAMPLE 3 Continuous Steam Stripping
Several commercially available emulsion polymers were continuously stripped using two different sets of stripping equipment. The first set of equipment was a Buffalo Technologies Corporation falling film stripper. The column had an internal diameter of 5.1 cm and a length of 3.7 m. The emulsion polymers were fed down the column while steam was fed up the column. Stripping was performed both under vacuum and at atmospheric pressure (Wet Air Stripping). The polymers were measured for VOCs by Gas Chromatography both before and after stripping. VOCs with boiling points below 100° C. were combined and reported together, as were VOCs with boiling points above 100° C. The samples were also passed through a 325 mesh screen to test for gel formation. The results of these experiments are shown in Table 3.
TABLE 3
Polymer Steam Column Temp. (° C.) VOCs
Example (kg/hr) (kg/hr) Top Bottom <100° C. >100° C. Gel
 1 A/16 6 52 51 160 320 No
 2 A/9 7 52 50  65 215 No
 3 A/29 5 52 51 130 258 No
 4 A/9 5 52 51 257 246 No
 5 A/41 5 50 50 205 281 120
 6 A/37 5 50 49 294 296 No
 7 A/46 6 51 49 120 259 103
 8 A/30 6 51 49 207 284 No
 9 A/37 6 49 49  97 236 No
10 B/11 5 49 48  69 260 B
11 B/19 9 49 48  58 308 B
12 (WA) B/51 19  33 31  580*  919* B
WA = wet air stripping
*experimental error suspected
Gel reported in parts per million
B = binded
The initial VOC levels for polymer A were 1342 ppm with a boiling point <100 ° C. and 432 ppm with a boiling point >100° C. The initial VOC levels for polymer B were 477 ppm with a boiling point <100° C., and 605 ppm with a boiling point >100° C. The examples above show that the continuous process utilizing the Buffalo Technologies Corporation falling film column removed VOCs from the polymer dispersion and did not form gel.
The second set of equipment was an Artisan Industries Corporation tube/disk falling film stripper. The column had an internal diameter of 10.2 cm and a length of 3.7 m. The emulsion polymers were fed down the column while steam was fed up the column. Stripping was performed both under vacuum and Wet Air Stripping. The polymers were analyzed as described above. The results of these experiments are shown in Table 4.
TABLE 4
Polymer Steam Column Temp. (° C.) VOCs
Example (kg/hr) (kg/hr) Top Bottom <100° C. >100° C. Gel
13 A/18 1 49 52 345 300 No
14 A/18 1 48 49 531 366 No
15 A/18 1 46 48 420 355 No
16 A/18 2 51 52  90 251 No
17 A/18 2 49 50  86 231 No
18 A/18 2 47 48  90 269 No
19 A/18 2.5 51 53  48 204 No
20 A/18 2.4 49 51  25 158 No
21 A/18 2.6 48 49  29 173 No
22 B/18 1.4 59 59  83 358 No
23 B/18 2.6 59 59  64 310 No
24 B/18 4.3 59 60  41 277 No
25 (WA) B/18 6.5 49 44 274 553 No
WA = wet air stripping
The initial VOC levels for polymer A were 1541 ppm with a boiling point <100° C., and 484 ppm with a boiling point >100° C. The initial VOC levels for polymer B were 470 ppm with a boiling point <100° C., and 588 ppm with a boiling point >100° C. The examples above show that the continuous process utilizing the Artisan Industries Corporation tube/disk falling film stripper removed VOCs from the polymer dispersion and did not form gel.

Claims (16)

We claim:
1. A process comprising:
providing a reaction composition comprising an aqueous emulsion polymer and stripping the reaction composition in the presence of a mechanical foam breaker and an agitator; wherein the reaction composition is treated by:
(a) adjusting the pH to from 7 to 11 prior to stripping and maintaining the adjusted pH during stripping and
(b) maintaining the temperature of the reaction composition at from 30° C. to 70° C. during stripping;
wherein the formation of gel is minimized.
2. The process according to claim 1 wherein, the pH of the reaction composition is adjusted to from 8 to 11 prior to stripping and maintained during stripping.
3. The process according to claim 1 wherein, the pH of the reaction composition is adjusted to from 8.5 to 11 prior to stripping and maintained during stripping.
4. The process according to claim 1 wherein, the temperature of the reaction composition is maintained at from 40° C. to 70° C. during stripping.
5. The process according to claim 1 wherein, the temperature of the reaction composition is maintained at from 45° C. to 59° C. during stripping.
6. The process according to claim 1 wherein, the pH of the reaction composition is adjusted to from 9 to 11 prior to stripping and maintained during stripping and the temperature of the reaction composition is maintained at from 45° C. to 59° C. during stripping.
7. The process according to claim 1 wherein, the agitator pumps the reaction composition up in the reactor.
8. The process according to claim 1 wherein, the reaction composition is chased with a chemical chaser selected from the group consisting of redox system combinations, inisurfs, and nucleophiles prior to stripping.
9. A process comprising:
i) continuously feeding a reaction composition comprising an acrylic dispersion polymer containing volatile organic compounds down a stripping column having a top and a bottom;
ii) continuously feeding steam up from the bottom of the stripping column; and
iii) removing the volatile organic compounds from the reaction composition;
wherein the pH of the reaction composition is adjusted to from 7 to 11 prior to stripping and maintaining the adjusted pH during stripping.
10. The process according to claim 9 wherein, the column flux rate of the reaction composition into the column ranges from 2,500 kg per hour per m2 to 30,000 kg per hour per m2 and the column flux rate of steam into the column ranges from 500 kg per hour per m2 to 12,500 kg per hour per m2.
11. The process according to claim 9 wherein, the stripping is performed at a temperature from 30° C. to 70° C. and a pressure from 20 mmHg to 150 mmHg.
12. The process according to claim 9 wherein, the pH of the reaction composition is adjusted to from 8 to 11 prior to stripping and maintained during stripping.
13. The process according to claim 9 wherein, the temperature of the reaction composition is maintained at from 40° C. to 70° C. during stripping.
14. The process according to claim 9 wherein, the pH of the reaction composition is adjusted to from 8.5 to 11 prior to stripping and maintained during stripping and the temperature of the reaction composition is maintained at from 45° C. to 59° C. during stripping.
15. The process according to claim 9 wherein, the reaction composition is chased with a chemical chaser selected from the group consisting of redox system combinations, inisurfs, and nucleophiles prior to stripping.
16. A process comprising providing a reaction composition comprising an aqueous emulsion polymer and stripping the reaction composition in the presence of a mechanical foam breaker and an agitator; wherein the reaction composition is treated by adjusting the pH to from 7 to 11 prior to stripping and maintaining the adjusted pH during stripping, wherein the formation of gel is minimized.
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Cited By (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20040143053A1 (en) * 2003-01-21 2004-07-22 Wu Richard Shu-Hua Process for preparing emulsion polymers
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US20060089454A1 (en) * 2004-10-21 2006-04-27 Ho-Yeul Choi Method for preparing styrene-butadiene latex
US20080103289A1 (en) * 2006-10-30 2008-05-01 Rohm & Haas Process for stripping polymer dispersions
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BR112022004476A2 (en) * 2019-09-30 2022-05-31 Dow Global Technologies Llc Process for pickling an aqueous dispersion of polymeric granules, and aqueous polymer composition

Citations (18)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1248943B (en) 1965-07-20 1967-08-31 Basf Ag Process and device for the discontinuous removal of odorous substances from aqueous polymer dispersions
US4016128A (en) * 1975-05-23 1977-04-05 Monsanto Company Preparation of aqueous solutions of quaternary ammonium resins from di(tertiary amine) and 1,4-dihalobutene-2
US4130527A (en) 1977-12-29 1978-12-19 Stauffer Chemical Company Method of treating a polymer latex to remove unreacted monomer by treatment in a column
US4132699A (en) * 1976-01-28 1979-01-02 British Steel Corporation (Chemicals) Ltd. Phenol formaldehyde resins, their manufacture and use
US4193903A (en) * 1978-05-17 1980-03-18 Standard Oil Company Rapid removal of residual monomers from acrylonitrile copolymers
US4197399A (en) * 1974-08-14 1980-04-08 Solvay & Cie Process for removing residual vinyl chloride from vinyl chloride polymers in aqueous dispersion
US4197400A (en) * 1974-11-25 1980-04-08 Solvay & Cie Process for removing monomer residues from acrylonitrile polymers
US4245073A (en) * 1975-05-26 1981-01-13 Solvay & Cie. Process for the polymerization of vinyl chloride in aqueous suspension
US4252705A (en) * 1978-12-26 1981-02-24 Argus Chemical Corporation Resistance of polyvinyl chloride resins to discoloration during drying with N,N'-diphenyl urea
US4292424A (en) * 1980-03-03 1981-09-29 The B.F. Goodrich Company Process for recovering vinyl polymers from emulsion polymerization latices
DE3123300A1 (en) 1981-06-12 1983-01-05 Basf Ag, 6700 Ludwigshafen Process for recovering unreacted vinyl chloride from strongly foaming polyvinyl chloride dispersions and polyvinyl chloride suspensions
US5194583A (en) * 1991-04-26 1993-03-16 Morton International, Inc. Method for neutralizing an alkaline solution of an organic resin
US5393856A (en) * 1993-08-11 1995-02-28 Amoco Corporation Liquid phase and aqueous solutions of poly(vinyl methyl ether) from highly purified vinyl methyl ether monomer
US5516818A (en) * 1994-09-26 1996-05-14 The Goodyear Tire & Rubber Company Method for removing small amounts of high boiling point organic compound from aqueous polymerization products
DE19517680A1 (en) 1995-05-13 1996-11-14 Buna Sow Leuna Olefinverb Gmbh Suppressing foaming during removal of free monomers from styrene butadiene latex
US5756659A (en) * 1991-03-04 1998-05-26 The Dow Chemical Company Method of improving the oxidative thermal stability of ethylene polymers
EP0865811A1 (en) 1997-03-17 1998-09-23 Basf Aktiengesellschaft Foam breaking process in the production of polymer dispersions
US6174991B1 (en) * 1996-12-31 2001-01-16 Bayer Inc. Process for making stabilized non-colored rubber

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE19741184A1 (en) * 1997-09-18 1999-03-25 Basf Ag Reducing residual monomer content of e.g. acrylic polymers

Patent Citations (18)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1248943B (en) 1965-07-20 1967-08-31 Basf Ag Process and device for the discontinuous removal of odorous substances from aqueous polymer dispersions
US4197399A (en) * 1974-08-14 1980-04-08 Solvay & Cie Process for removing residual vinyl chloride from vinyl chloride polymers in aqueous dispersion
US4197400A (en) * 1974-11-25 1980-04-08 Solvay & Cie Process for removing monomer residues from acrylonitrile polymers
US4016128A (en) * 1975-05-23 1977-04-05 Monsanto Company Preparation of aqueous solutions of quaternary ammonium resins from di(tertiary amine) and 1,4-dihalobutene-2
US4245073A (en) * 1975-05-26 1981-01-13 Solvay & Cie. Process for the polymerization of vinyl chloride in aqueous suspension
US4132699A (en) * 1976-01-28 1979-01-02 British Steel Corporation (Chemicals) Ltd. Phenol formaldehyde resins, their manufacture and use
US4130527A (en) 1977-12-29 1978-12-19 Stauffer Chemical Company Method of treating a polymer latex to remove unreacted monomer by treatment in a column
US4193903A (en) * 1978-05-17 1980-03-18 Standard Oil Company Rapid removal of residual monomers from acrylonitrile copolymers
US4252705A (en) * 1978-12-26 1981-02-24 Argus Chemical Corporation Resistance of polyvinyl chloride resins to discoloration during drying with N,N'-diphenyl urea
US4292424A (en) * 1980-03-03 1981-09-29 The B.F. Goodrich Company Process for recovering vinyl polymers from emulsion polymerization latices
DE3123300A1 (en) 1981-06-12 1983-01-05 Basf Ag, 6700 Ludwigshafen Process for recovering unreacted vinyl chloride from strongly foaming polyvinyl chloride dispersions and polyvinyl chloride suspensions
US5756659A (en) * 1991-03-04 1998-05-26 The Dow Chemical Company Method of improving the oxidative thermal stability of ethylene polymers
US5194583A (en) * 1991-04-26 1993-03-16 Morton International, Inc. Method for neutralizing an alkaline solution of an organic resin
US5393856A (en) * 1993-08-11 1995-02-28 Amoco Corporation Liquid phase and aqueous solutions of poly(vinyl methyl ether) from highly purified vinyl methyl ether monomer
US5516818A (en) * 1994-09-26 1996-05-14 The Goodyear Tire & Rubber Company Method for removing small amounts of high boiling point organic compound from aqueous polymerization products
DE19517680A1 (en) 1995-05-13 1996-11-14 Buna Sow Leuna Olefinverb Gmbh Suppressing foaming during removal of free monomers from styrene butadiene latex
US6174991B1 (en) * 1996-12-31 2001-01-16 Bayer Inc. Process for making stabilized non-colored rubber
EP0865811A1 (en) 1997-03-17 1998-09-23 Basf Aktiengesellschaft Foam breaking process in the production of polymer dispersions

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
American Laboratory, Mar. 1989, "A mechanical Foam Separator For Industrial Chemical Processing" by R. B. Roy.

Cited By (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20040143053A1 (en) * 2003-01-21 2004-07-22 Wu Richard Shu-Hua Process for preparing emulsion polymers
US20050107581A1 (en) * 2003-11-17 2005-05-19 Bruce Rosenbaum Process for the removal of porogens from temperature sensitive macroreticular polymers using steam at reduced pressure
US20060089454A1 (en) * 2004-10-21 2006-04-27 Ho-Yeul Choi Method for preparing styrene-butadiene latex
US7612128B2 (en) * 2004-10-21 2009-11-03 Lg Chem, Ltd. Method for preparing styrene-butadiene latex
US20080103289A1 (en) * 2006-10-30 2008-05-01 Rohm & Haas Process for stripping polymer dispersions
US7745567B2 (en) * 2006-10-30 2010-06-29 Rohm And Haas Company Process for stripping polymer dispersions
US20110098376A1 (en) * 2008-06-13 2011-04-28 Sheerin Robert J Aqueous Coating Compositions with De Minimis Volatile Emissions
US8507579B2 (en) 2008-06-13 2013-08-13 Columbia Insurance Company Aqueous coating compositions with de minimis volatile emissions
WO2011141176A1 (en) * 2010-05-14 2011-11-17 List Holding Ag Method for carrying out polymerisation processes
RU2575177C2 (en) * 2010-05-14 2016-02-20 Лист Холдинг АГ Method for realisation of polymerisation processes
US8771523B1 (en) * 2013-01-29 2014-07-08 Xerox Corporation Polydisperse compositions and methods for eliminating volatile organic compounds
US20160052858A1 (en) * 2014-08-21 2016-02-25 Abraham Joy Alkyl alpha-hydroxymethyl acrylates as reactive surfactants in emulsion polymerization
US10118887B2 (en) * 2014-08-21 2018-11-06 The University Of Akron Alkyl alpha-hydroxymethyl acrylates as reactive surfactants in emulsion polymerization
US11642660B2 (en) * 2015-11-05 2023-05-09 Nikki-Universal Co., Ltd. Purification catalyst for interior of polymer film production furnace and purification method for interior of polymer film production furnace
WO2021126488A1 (en) 2019-12-17 2021-06-24 Benjamin Moore & Co. Redox chased suspension bead additives for paints and stains

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EP1078936A3 (en) 2001-07-18
DE60015672T2 (en) 2005-12-01
EP1078936B1 (en) 2004-11-10
BR0003800A (en) 2001-04-03
TWI232224B (en) 2005-05-11
JP2001098012A (en) 2001-04-10
KR20010050090A (en) 2001-06-15
AU5341200A (en) 2001-03-01
CN1495224A (en) 2004-05-12
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CN1286270A (en) 2001-03-07
EP1078936A2 (en) 2001-02-28

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